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FDA 510(k)

WILLIAMS-FRITTS PLEURAL BIOPSY NEEDLE

K-Number: K883876 · 1988-10-07

ApplicantE.G. Dick & Assoc.
Decision Date1988-10-07
Product CodeGDM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

WILLIAMS-FRITTS PLEURAL BIOPSY NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is E.G. Dick & Assoc.. It received FDA 510(k) clearance on 1988-10-07 under 510(k) number K883876. The device is classified under product code GDM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WILLIAMS-FRITTS PLEURAL BIOPSY NEEDLE?

WILLIAMS-FRITTS PLEURAL BIOPSY NEEDLE is a medical device that received FDA 510(k) clearance on 1988-10-07. The listed applicant is E.G. Dick & Assoc.. The 510(k) number is K883876.

When did WILLIAMS-FRITTS PLEURAL BIOPSY NEEDLE receive FDA 510(k) clearance?

WILLIAMS-FRITTS PLEURAL BIOPSY NEEDLE received FDA 510(k) clearance on 1988-10-07, under 510(k) number K883876.

Who is the listed applicant for WILLIAMS-FRITTS PLEURAL BIOPSY NEEDLE?

The FDA 510(k) record lists E.G. Dick & Assoc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WILLIAMS-FRITTS PLEURAL BIOPSY NEEDLE?

The FDA product code for WILLIAMS-FRITTS PLEURAL BIOPSY NEEDLE is GDM.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing E.G. Dick & Assoc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K881624PLEURAL BIOPSY PUNCH NEEDLEK881854SORBSAN TOPICAL WOUND DRESSING

Related Devices (Code: GDM)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K071732MARROWMINERStemcor Systems, Inc.K971114BIOACCESS MARROW HARVEST SYSTEMBioaccess, Inc.K953082ILIAC CREST BONE MARROW ASPIRATION NEEDLEBaxter Healthcare CorpK953064BIOACCESS MARROW HARVEST SYSTEMBioaccess, Inc.K936207ENDO-NEEDLE INSTRUMENTGerard Medical, Inc.K930160ILLINOIS STERNAL/ILIAC ASPIRATION NEEDLESymbiosis Corp.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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